Martin DM - Search Results

1

CHD7 and SOX2 act in a common gene regulatory network during mammalian semicircular canal and cochlear development.

Gao J, Skidmore JM, Cimerman J, Ritter KE, Qiu J, Wilson LMQ, Raphael Y, Kwan KY, Martin DM. Gao J, et al. Among authors: martin dm. Proc Natl Acad Sci U S A. 2024 Mar 5;121(10):e2311720121. doi: 10.1073/pnas.2311720121. Epub 2024 Feb 26. Proc Natl Acad Sci U S A. 2024. PMID: 38408234

2

Chromatin remodeler CHD7 is critical for cochlear morphogenesis and neurosensory patterning.

Balendran V, Skidmore JM, Ritter KE, Gao J, Cimerman J, Beyer LA, Hurd EA, Raphael Y, Martin DM. Balendran V, et al. Among authors: martin dm. Dev Biol. 2021 Sep;477:11-21. doi: 10.1016/j.ydbio.2021.05.009. Epub 2021 May 15. Dev Biol. 2021. PMID: 34004180 Free PMC article.

3

Have you heard? Viral-mediated gene therapy restores hearing.

Martin DM, Raphael Y. Martin DM, et al. Neuron. 2012 Jul 26;75(2):188-90. doi: 10.1016/j.neuron.2012.06.008. Neuron. 2012. PMID: 22841304 Free PMC article.

4

CHD7 represses the retinoic acid synthesis enzyme ALDH1A3 during inner ear development.

Yao H, Hill SF, Skidmore JM, Sperry ED, Swiderski DL, Sanchez GJ, Bartels CF, Raphael Y, Scacheri PC, Iwase S, Martin DM. Yao H, et al. Among authors: martin dm. JCI Insight. 2018 Feb 22;3(4):e97440. doi: 10.1172/jci.insight.97440. eCollection 2018 Feb 22. JCI Insight. 2018. PMID: 29467333 Free PMC article.

5

Neural crest contributions to the ear: Implications for congenital hearing disorders.

Ritter KE, Martin DM. Ritter KE, et al. Among authors: martin dm. Hear Res. 2019 May;376:22-32. doi: 10.1016/j.heares.2018.11.005. Epub 2018 Nov 14. Hear Res. 2019. PMID: 30455064 Free PMC article. Review.

6

GJB2 gene therapy and conditional deletion reveal developmental stage-dependent effects on inner ear structure and function.

Guo J, Ma X, Skidmore JM, Cimerman J, Prieskorn DM, Beyer LA, Swiderski DL, Dolan DF, Martin DM, Raphael Y. Guo J, et al. Among authors: martin dm. Mol Ther Methods Clin Dev. 2021 Oct 1;23:319-333. doi: 10.1016/j.omtm.2021.09.009. eCollection 2021 Dec 10. Mol Ther Methods Clin Dev. 2021. PMID: 34729379 Free PMC article.

7

Epigenetic mechanisms of inner ear development.

Balendran V, Ritter KE, Martin DM. Balendran V, et al. Among authors: martin dm. Hear Res. 2022 Dec;426:108440. doi: 10.1016/j.heares.2022.108440. Epub 2022 Jan 13. Hear Res. 2022. PMID: 35063312 Free PMC article. Review.

8

Gene-based diagnostic and treatment methods for tinnitus.

Martin DM, Raphael Y. Martin DM, et al. Int Tinnitus J. 2003;9(1):3-10. Int Tinnitus J. 2003. PMID: 14763322 Review.

9

Cre fate mapping reveals lineage specific defects in neuronal migration with loss of Pitx2 function in the developing mouse hypothalamus and subthalamic nucleus.

Skidmore JM, Cramer JD, Martin JF, Martin DM. Skidmore JM, et al. Among authors: martin jf, martin dm. Mol Cell Neurosci. 2008 Apr;37(4):696-707. doi: 10.1016/j.mcn.2007.12.015. Epub 2007 Dec 15. Mol Cell Neurosci. 2008. PMID: 18206388 Free PMC article.

10

The ATP-dependent chromatin remodeling enzyme CHD7 regulates pro-neural gene expression and neurogenesis in the inner ear.

Hurd EA, Poucher HK, Cheng K, Raphael Y, Martin DM. Hurd EA, et al. Among authors: martin dm. Development. 2010 Sep;137(18):3139-50. doi: 10.1242/dev.047894. Development. 2010. PMID: 20736290 Free PMC article.

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